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1دورية أكاديمية
المؤلفون: James Anthony Davies, Derrick John Bowen
المصدر: Haematologica, Vol 92, Iss 2 (2007)
مصطلحات موضوعية: Diseases of the blood and blood-forming organs, RC633-647.5
وصف الملف: electronic resource
العلاقة: https://haematologica.org/article/view/4331Test; https://doaj.org/toc/0390-6078Test; https://doaj.org/toc/1592-8721Test
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المصدر: Molecular Immunology. 52:88-95
مصطلحات موضوعية: Untranslated region, Amino Acid Motifs, Immunology, Codon, Initiator, Biology, Transfection, Monocytes, C5a receptor, Mice, Species Specificity, Animals, Humans, Cloning, Molecular, Promoter Regions, Genetic, Site-directed mutagenesis, 3' Untranslated Regions, Receptor, Anaphylatoxin C5a, Molecular Biology, AU-rich element, Messenger RNA, Binding Sites, Base Sequence, NFATC Transcription Factors, Three prime untranslated region, NF-kappa B, Cell Differentiation, Promoter, U937 Cells, Molecular biology, Recombinant Proteins, Receptors, Complement, Bucladesine, CCAAT-Binding Factor, Gene Expression Regulation, Regulatory sequence, Mutagenesis, Site-Directed, Tetradecanoylphorbol Acetate
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::12d09fe4b55315726324e47fdafa0421Test
https://doi.org/10.1016/j.molimm.2012.04.012Test -
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المؤلفون: A. M. Cumming, M. Bowman, Stephen Keeney, Charles R. M. Hay, Megan Sutherland, Andrew M. Will, Derrick John Bowen, Peter William Collins, Paula H. B. Bolton-Maggs
المصدر: Blood. 114:1091-1098
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Adolescent, Genotype, Recombinant Fusion Proteins, Immunology, Biology, Compound heterozygosity, medicine.disease_cause, Biochemistry, White People, Young Adult, Exon, Asian People, hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Aged, Genes, Dominant, Sequence Deletion, Aged, 80 and over, Genetics, Mutation, Haplotype, Heterozygote advantage, Exons, Sequence Analysis, DNA, Cell Biology, Hematology, Middle Aged, medicine.disease, Founder Effect, von Willebrand Diseases, genomic DNA, England, Haplotypes, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::087bb2e657c641a0bf4cdfa7fc41542fTest
https://doi.org/10.1182/blood-2008-08-173278Test -
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المؤلفون: A. M. Cumming, Said Enayat, M. Hill, Anne Goodeve, Derrick John Bowen, S. Keeney
المصدر: Haemophilia. 14:1099-1111
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Genetic Linkage, DNA Mutational Analysis, Haemophilia, Von Willebrand factor, Pregnancy, Genetic linkage, Prenatal Diagnosis, Terminology as Topic, hemic and lymphatic diseases, von Willebrand Factor, medicine, Von Willebrand disease, Humans, Genetics (clinical), Genetics, biology, Molecular pathology, business.industry, Hematology, General Medicine, Guideline, medicine.disease, Penetrance, Fetal Diseases, von Willebrand Diseases, Coagulation, Mutation, Immunology, biology.protein, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d6d0400fd78bda2d1f9dcc50817f248Test
https://doi.org/10.1111/j.1365-2516.2008.01813.xTest -
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المؤلفون: Jeanne Kingston, Mark Worwood, Susan Lawless, Helen A. Jackson, Derrick John Bowen, Marion Carol Sweeney
المصدر: Journal of Clinical Pathology. 60:1244-1248
مصطلحات موضوعية: medicine.medical_specialty, Population, Heteroduplex Analysis, Biology, Compound heterozygosity, Polymerase Chain Reaction, Pathology and Forensic Medicine, Gene Frequency, Internal medicine, Genotype, medicine, Humans, Genetic Testing, Hemochromatosis Protein, education, Allele frequency, Hemochromatosis, Genetic testing, Genetics, education.field_of_study, medicine.diagnostic_test, Transferrin saturation, Histocompatibility Antigens Class I, Electrophoresis, Capillary, Membrane Proteins, Reproducibility of Results, General Medicine, medicine.disease, Genotype frequency, Original Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d7735d6be7337ee776307490eedc7ea3Test
https://doi.org/10.1136/jcp.2006.042010Test -
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المؤلفون: Derrick John Bowen, Peter William Collins
المصدر: British Journal of Haematology. 133:457-467
مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Thrombospondin, medicine.medical_specialty, Hematology, medicine.diagnostic_test, biology, business.industry, Proteolysis, Thrombotic thrombocytopenic purpura, medicine.disease, ADAMTS13, Von Willebrand factor, hemic and lymphatic diseases, Internal medicine, Immunology, Von Willebrand disease, medicine, Disintegrin, biology.protein, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::9d1436d169abe02cac2a9ec85ece9b5eTest
https://doi.org/10.1111/j.1365-2141.2006.06096.xTest -
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المؤلفون: M. A. Haj, Derrick John Bowen, H. I. Sati, Peter William Collins, N. Murch, A. Benton, A. Beddal
المصدر: European Journal of Haematology. 76:440-443
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pathology, Cefotaxime, medicine.drug_class, Cephalosporin, Plasma cell, Gastroenterology, Dyscrasia, Surgical prophylaxis, Acquired von Willebrand syndrome, Myeloproliferative Disorders, Internal medicine, medicine, Humans, business.industry, Hematology, General Medicine, von Willebrand Diseases, Treatment Outcome, medicine.anatomical_structure, Bacterial meningitis, business, Follow-Up Studies, medicine.drug
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2edcf9385243ea4d3b74a3b27ee32501Test
https://doi.org/10.1111/j.0902-4441.2006.t01-1-ejh2386.xTest -
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المؤلفون: Charles R. M. Hay, Frank Hill, Andrea Guilliatt, Peter William Collins, Pamela Grundy, William Lester, Derrick John Bowen, A. M. Cumming, Stephen Keeney, Said Enayat, John Pasi, Paula H B Bolton-Maggs, David Keeling
المصدر: Thrombosis and Haemostasis. 96:630-641
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Genotype, Genetic Linkage, DNA Mutational Analysis, Penetrance, Biology, Gene mutation, medicine.disease_cause, Von Willebrand factor, Polymorphism (computer science), hemic and lymphatic diseases, von Willebrand Factor, Von Willebrand disease, medicine, Humans, Family Health, Genetics, Mutation, Polymorphism, Genetic, Haplotype, Hematology, medicine.disease, United Kingdom, Pedigree, von Willebrand Diseases, Haplotypes, Immunology, biology.protein, Female
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::49fb43623c88217b1da3de19baf9c78cTest
https://doi.org/10.1160/th06-07-0383Test -
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المؤلفون: R. Campbell Tait, Will Lester, Jonathon T. Wilde, Derrick John Bowen, Frank Hill, Kate Khair, A. M. Cumming, K. John Pasi, Peter William Collins, Pamela Grundy, Paula H. B. Bolton-Maggs, Steven Keeney, David Keeling, Saad M. Enayat
المصدر: British Journal of Haematology. 128:830-836
مصطلحات موضوعية: Male, Heterozygote, congenital, hereditary, and neonatal diseases and abnormalities, ADAMTS13 Protein, Enzyme-Linked Immunosorbent Assay, Haemophilia, ABO Blood-Group System, Cohort Studies, Von Willebrand factor, Polymorphism (computer science), hemic and lymphatic diseases, ABO blood group system, medicine, Von Willebrand disease, Coagulopathy, Humans, Genetic Predisposition to Disease, Cysteine, Polymorphism, Genetic, biology, business.industry, ADAMTS, Metalloendopeptidases, Hematology, medicine.disease, ADAMTS13, Pedigree, ADAM Proteins, von Willebrand Diseases, Phenotype, Immunology, biology.protein, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b0ce53ea386ad0e8235ea25ddec826bTest
https://doi.org/10.1111/j.1365-2141.2005.05375.xTest -
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المصدر: British Journal of Haematology. 126:602-605
مصطلحات موضوعية: Genetics, Neuroblastoma RAS viral oncogene homolog, Mutation, Hematology, Biology, Gene mutation, medicine.disease_cause, Molecular biology, Exon, Multiplex polymerase chain reaction, medicine, Multiplex, Routine analysis, Heteroduplex
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::151f996b88c327e7b473999e7b3cd259Test
https://doi.org/10.1111/j.1365-2141.2004.05079.xTest